重氮甲烷
磷化氢
量子产额
量子点
光致发光
半最大全宽
化学
成核
产量(工程)
特里斯
反应性(心理学)
纳米技术
材料科学
光电子学
物理
有机化学
催化作用
光学
荧光
冶金
病理
替代医学
医学
生物化学
作者
Doheon Yoo,Euk Hyun Kim,Ji‐Seoung Jeong,Ji Yeon Ryu,Sang Man Koo,Min‐Jae Choi
标识
DOI:10.1002/anie.202513545
摘要
Abstract Aminophosphines have emerged as promising phosphorus candidates for the synthesis of InP quantum dots (QDs), offering an alternative to traditional tris(trimethylsilyl) phosphine. However, the relatively low reactivity of conventional aminophosphines has led to broader size distribution, resulting in higher full‐width at half‐maximum (FHWM) with lower photoluminescence quantum yield (PLQY). Here, we introduce a new aminosphosphine, bis(bis(trimethylsilyl)amino) phosphine (P[N(SiMe 3 ) 2 ] 2 H), to address this issue. Using nuclear magnetic resonance (NMR) spectroscopy, we demonstrate the direct nucleophilic activation of the P[N(SiMe 3 ) 2 ] 2 H with InCl 3 , leading to the rapid nucleation of InP QDs at a relatively lower synthesis temperature. This enabled to achieve InP/ZnSeS/ZnS QDs with near‐unity PLQY and a FWHM of 48 nm. These findings suggest a new chemistry for the synthesis of InP QDs, and could be extended to other III‐V QDs for advanced optoelectronic applications.
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